LiNi
x
Mn2
-
x
O4 (x ≤ 0.5) powders were synthesized using a sol−gel technique. It was found that partial Ni
atoms occupy the 8a sites in heavy doped LiNi
x
Mn2
-
x
O4 via X-ray diffraction. XPS results showed an increase
and a decrease in the average valence state of Mn and Ni ions, respectively, with the nickel content. Five
Raman modes of LiNi
x
Mn2
-
x
O4 were observed. The A1g band was observed being shifted to higher frequency
for x ≤ 0.2 and shifted to lower frequency for x > 0.2. It was indicated that the most rigid [MnO6] octahedron
occurs at x = 0.2. [MnO6] octahedron in LiNi0.2Mn1.8O4 possesses the strongest rigidity with respect to the
other LiNi
x
Mn2
-
x
O4 (x < 0.5 and ≠ 0.2).
Structures of Si
n
O
n
clusters are of great interest because of the observed growth of oxide-coated Si nanowires
from gas-phase SiO. We studied the geometries of Si
n
O
n
clusters with n ranging from 12 to 18 using first-principles density functional calculations. We found a new structural motif which produces structures that
are energetically more favorable than those proposed in recent literature. These structures consist of polygonal
bipyramidal Si clusters of sizes between 5 and 7 attached to low-energy Si8O12 or Si12O18 wheel structures
previously discovered. The segregation of silicon to the side of the cluster is intriguing and contradicts previous
models that assumed silicon segregation nucleates in the center of the monoxide clusters. Electronic structure
analysis shows that the HOMO and LUMO states of the monoxide clusters are localized on the segregated
silicon cluster, indicating that the segregated Si may act as a nucleation site for further nanostructure growth.
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